Name | Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Mitochondrial Diseases | 7 | 2018 | 342 | 0.910 |
Why?
|
Plasma Membrane Neurotransmitter Transport Proteins | 5 | 2020 | 23 | 0.650 |
Why?
|
Lissencephaly | 1 | 2016 | 36 | 0.550 |
Why?
|
Cytochrome Reductases | 1 | 2015 | 9 | 0.510 |
Why?
|
Atrophy | 1 | 2020 | 1633 | 0.480 |
Why?
|
Peptide Termination Factors | 1 | 2014 | 56 | 0.450 |
Why?
|
Acidosis, Lactic | 1 | 2015 | 146 | 0.440 |
Why?
|
Optic Atrophy | 1 | 2014 | 79 | 0.440 |
Why?
|
Adrenal Insufficiency | 1 | 2015 | 194 | 0.430 |
Why?
|
Leigh Disease | 1 | 2014 | 89 | 0.420 |
Why?
|
Tubulin | 1 | 2016 | 692 | 0.420 |
Why?
|
Angelman Syndrome | 4 | 2019 | 139 | 0.380 |
Why?
|
Siblings | 2 | 2016 | 824 | 0.360 |
Why?
|
Genetic Predisposition to Disease | 6 | 2021 | 17897 | 0.340 |
Why?
|
Dystonic Disorders | 2 | 2016 | 350 | 0.340 |
Why?
|
Genetic Variation | 5 | 2021 | 6567 | 0.330 |
Why?
|
Aromatic-L-Amino-Acid Decarboxylases | 2 | 2021 | 27 | 0.320 |
Why?
|
Cataract | 1 | 2015 | 828 | 0.320 |
Why?
|
Nerve Tissue Proteins | 5 | 2017 | 4404 | 0.300 |
Why?
|
Phenotype | 14 | 2021 | 16575 | 0.280 |
Why?
|
Ventricular Premature Complexes | 1 | 2008 | 112 | 0.280 |
Why?
|
Sodium-Potassium-Exchanging ATPase | 1 | 2009 | 476 | 0.270 |
Why?
|
Parkinsonian Disorders | 1 | 2009 | 285 | 0.270 |
Why?
|
MELAS Syndrome | 1 | 2006 | 56 | 0.260 |
Why?
|
Frameshift Mutation | 1 | 2008 | 392 | 0.260 |
Why?
|
Betaine | 2 | 2019 | 90 | 0.250 |
Why?
|
Mental Retardation, X-Linked | 4 | 2020 | 41 | 0.250 |
Why?
|
Mutation | 9 | 2021 | 30002 | 0.250 |
Why?
|
Muscle Hypotonia | 2 | 2020 | 161 | 0.230 |
Why?
|
Chromosomes, Human, X | 1 | 2006 | 320 | 0.220 |
Why?
|
Norepinephrine | 1 | 2006 | 897 | 0.220 |
Why?
|
Metabolism, Inborn Errors | 1 | 2006 | 284 | 0.220 |
Why?
|
Creatine | 4 | 2020 | 427 | 0.220 |
Why?
|
Cardiotonic Agents | 1 | 2006 | 540 | 0.210 |
Why?
|
Vasoconstrictor Agents | 1 | 2006 | 655 | 0.210 |
Why?
|
Carboxy-Lyases | 1 | 2021 | 85 | 0.190 |
Why?
|
Heterogeneous-Nuclear Ribonucleoproteins | 1 | 2021 | 69 | 0.180 |
Why?
|
Peripheral Nervous System Diseases | 1 | 2006 | 709 | 0.180 |
Why?
|
Brain Diseases, Metabolic, Inborn | 3 | 2020 | 46 | 0.180 |
Why?
|
Epilepsy | 4 | 2020 | 3304 | 0.180 |
Why?
|
Membrane Transport Proteins | 1 | 2006 | 1031 | 0.170 |
Why?
|
DNA | 1 | 2014 | 7189 | 0.170 |
Why?
|
Chromosomes, Human, Pair 15 | 3 | 2011 | 361 | 0.170 |
Why?
|
Developmental Disabilities | 1 | 2008 | 1510 | 0.160 |
Why?
|
Dopamine | 1 | 2006 | 1601 | 0.160 |
Why?
|
GTP-Binding Protein alpha Subunits, Gi-Go | 1 | 2019 | 89 | 0.160 |
Why?
|
Folic Acid | 2 | 2019 | 1323 | 0.160 |
Why?
|
Carbon-Nitrogen Ligases | 1 | 2018 | 27 | 0.160 |
Why?
|
Amino Acid Transport Systems, Acidic | 1 | 2018 | 30 | 0.150 |
Why?
|
Acyltransferases | 1 | 2020 | 304 | 0.150 |
Why?
|
Hereditary Central Nervous System Demyelinating Diseases | 1 | 2018 | 42 | 0.150 |
Why?
|
Cerebellar Diseases | 1 | 2020 | 220 | 0.150 |
Why?
|
Microcephaly | 2 | 2020 | 425 | 0.150 |
Why?
|
Craniofacial Abnormalities | 1 | 2020 | 319 | 0.150 |
Why?
|
Psychomotor Disorders | 1 | 2018 | 149 | 0.140 |
Why?
|
Succinate-CoA Ligases | 1 | 2016 | 6 | 0.140 |
Why?
|
Genetic Association Studies | 4 | 2021 | 2731 | 0.140 |
Why?
|
Apoptosis Inducing Factor | 1 | 2017 | 51 | 0.140 |
Why?
|
Mitochondrial Encephalomyopathies | 1 | 2017 | 40 | 0.140 |
Why?
|
Antiporters | 1 | 2018 | 276 | 0.140 |
Why?
|
Arrhythmias, Cardiac | 1 | 2006 | 2247 | 0.130 |
Why?
|
Heterozygote | 2 | 2020 | 2778 | 0.130 |
Why?
|
Charcot-Marie-Tooth Disease | 1 | 2017 | 100 | 0.130 |
Why?
|
Adenosine Triphosphatases | 1 | 2020 | 833 | 0.130 |
Why?
|
Hyperkinesis | 1 | 2016 | 88 | 0.130 |
Why?
|
Morocco | 1 | 2015 | 30 | 0.130 |
Why?
|
Oxidoreductases Acting on Sulfur Group Donors | 1 | 2015 | 32 | 0.130 |
Why?
|
Chorea | 1 | 2016 | 79 | 0.130 |
Why?
|
Growth Disorders | 1 | 2020 | 634 | 0.120 |
Why?
|
Child, Preschool | 12 | 2020 | 42224 | 0.110 |
Why?
|
Child | 19 | 2020 | 80152 | 0.110 |
Why?
|
Cell Adhesion Molecules | 1 | 2020 | 1603 | 0.110 |
Why?
|
Cholestasis, Intrahepatic | 1 | 2014 | 75 | 0.110 |
Why?
|
Sequence Deletion | 3 | 2019 | 1487 | 0.110 |
Why?
|
Standard of Care | 1 | 2017 | 550 | 0.110 |
Why?
|
Microfilament Proteins | 1 | 2018 | 1130 | 0.110 |
Why?
|
DNA Mutational Analysis | 2 | 2014 | 4107 | 0.110 |
Why?
|
Consanguinity | 1 | 2015 | 457 | 0.110 |
Why?
|
Chromosome Aberrations | 2 | 2011 | 1767 | 0.110 |
Why?
|
Psychometrics | 2 | 2020 | 3061 | 0.100 |
Why?
|
Brain Diseases, Metabolic | 1 | 2012 | 44 | 0.100 |
Why?
|
Rhabdomyolysis | 1 | 2012 | 152 | 0.090 |
Why?
|
ATP-Binding Cassette Transporters | 1 | 2014 | 563 | 0.090 |
Why?
|
Neuropsychological Tests | 2 | 2020 | 7046 | 0.090 |
Why?
|
Amino Acid Metabolism, Inborn Errors | 1 | 2012 | 283 | 0.080 |
Why?
|
Brain | 7 | 2021 | 27092 | 0.080 |
Why?
|
Dystonia | 1 | 2012 | 370 | 0.080 |
Why?
|
Humans | 34 | 2021 | 761208 | 0.080 |
Why?
|
Mitochondrial Proteins | 1 | 2014 | 974 | 0.070 |
Why?
|
Deep Brain Stimulation | 1 | 2016 | 829 | 0.070 |
Why?
|
Male | 22 | 2020 | 360693 | 0.070 |
Why?
|
Fatal Outcome | 2 | 2016 | 1838 | 0.070 |
Why?
|
Parkinson Disease | 1 | 2021 | 2867 | 0.070 |
Why?
|
Nervous System Malformations | 2 | 2020 | 244 | 0.070 |
Why?
|
Magnetic Resonance Spectroscopy | 2 | 2008 | 3770 | 0.070 |
Why?
|
Language Development Disorders | 1 | 2008 | 193 | 0.070 |
Why?
|
Peroneal Nerve | 1 | 2006 | 76 | 0.070 |
Why?
|
Sural Nerve | 1 | 2006 | 105 | 0.070 |
Why?
|
Carrier Proteins | 1 | 2018 | 4935 | 0.060 |
Why?
|
Mitochondria | 2 | 2017 | 3620 | 0.060 |
Why?
|
Electrocardiography, Ambulatory | 1 | 2008 | 577 | 0.060 |
Why?
|
Neural Conduction | 1 | 2006 | 441 | 0.060 |
Why?
|
Infant | 9 | 2020 | 36169 | 0.060 |
Why?
|
Amino Acid Substitution | 1 | 2009 | 1737 | 0.060 |
Why?
|
Glycine | 1 | 2008 | 659 | 0.060 |
Why?
|
Muscle, Skeletal | 2 | 2017 | 4947 | 0.060 |
Why?
|
Brain Chemistry | 1 | 2008 | 959 | 0.060 |
Why?
|
Ubiquitin-Protein Ligases | 2 | 2011 | 1892 | 0.060 |
Why?
|
Vasculitis, Central Nervous System | 1 | 2004 | 45 | 0.060 |
Why?
|
Family | 1 | 2015 | 3192 | 0.060 |
Why?
|
Adolescent | 7 | 2020 | 88298 | 0.060 |
Why?
|
Deglutition Disorders | 1 | 2009 | 627 | 0.050 |
Why?
|
Vitamin B Complex | 2 | 2019 | 299 | 0.050 |
Why?
|
Gene Deletion | 2 | 2014 | 2658 | 0.050 |
Why?
|
Child Behavior Disorders | 1 | 2008 | 804 | 0.050 |
Why?
|
Comparative Genomic Hybridization | 2 | 2018 | 473 | 0.050 |
Why?
|
Genetic Markers | 1 | 2009 | 2599 | 0.050 |
Why?
|
Age of Onset | 1 | 2009 | 3307 | 0.050 |
Why?
|
Exons | 1 | 2008 | 2380 | 0.050 |
Why?
|
Heart Arrest | 1 | 2012 | 1513 | 0.050 |
Why?
|
Double-Blind Method | 3 | 2019 | 12341 | 0.050 |
Why?
|
Eye | 1 | 2006 | 713 | 0.050 |
Why?
|
Female | 13 | 2020 | 392544 | 0.050 |
Why?
|
DNA, Mitochondrial | 2 | 2017 | 865 | 0.050 |
Why?
|
Polymorphism, Single Nucleotide | 2 | 2018 | 15920 | 0.040 |
Why?
|
Transcription Factors | 1 | 2020 | 12099 | 0.040 |
Why?
|
Putamen | 1 | 2021 | 292 | 0.040 |
Why?
|
Cross-Over Studies | 1 | 2006 | 2082 | 0.040 |
Why?
|
DNA Methylation | 2 | 2011 | 4384 | 0.040 |
Why?
|
Acute Kidney Injury | 1 | 2012 | 1923 | 0.040 |
Why?
|
Action Potentials | 1 | 2006 | 1830 | 0.040 |
Why?
|
Progeria | 1 | 2001 | 188 | 0.040 |
Why?
|
Autistic Disorder | 1 | 2008 | 1222 | 0.040 |
Why?
|
Inheritance Patterns | 1 | 2021 | 341 | 0.040 |
Why?
|
Genotype | 2 | 2013 | 12985 | 0.040 |
Why?
|
Acute Disease | 1 | 2009 | 7226 | 0.040 |
Why?
|
Dietary Supplements | 1 | 2011 | 3410 | 0.040 |
Why?
|
RNA Processing, Post-Transcriptional | 1 | 2021 | 394 | 0.040 |
Why?
|
Neuroaxonal Dystrophies | 1 | 2018 | 26 | 0.040 |
Why?
|
Folate Receptor 1 | 1 | 2018 | 40 | 0.040 |
Why?
|
Tetrahydrofolates | 1 | 2018 | 58 | 0.040 |
Why?
|
Facies | 1 | 2018 | 222 | 0.040 |
Why?
|
Twins, Monozygotic | 1 | 2019 | 470 | 0.040 |
Why?
|
Young Adult | 4 | 2020 | 59221 | 0.040 |
Why?
|
Epilepsies, Partial | 1 | 2001 | 431 | 0.040 |
Why?
|
Base Sequence | 1 | 2008 | 12404 | 0.030 |
Why?
|
Membrane Proteins | 1 | 2014 | 7851 | 0.030 |
Why?
|
Electron Transport | 1 | 2017 | 209 | 0.030 |
Why?
|
Cerebral Infarction | 1 | 2001 | 981 | 0.030 |
Why?
|
Genetic Diseases, Inborn | 1 | 2020 | 603 | 0.030 |
Why?
|
Molecular Sequence Data | 1 | 2008 | 17598 | 0.030 |
Why?
|
Follow-Up Studies | 2 | 2014 | 39126 | 0.030 |
Why?
|
Physicians | 1 | 2013 | 4584 | 0.030 |
Why?
|
Phosphorylation | 1 | 2006 | 8300 | 0.030 |
Why?
|
Gastrointestinal Agents | 1 | 2019 | 509 | 0.030 |
Why?
|
Oxygen | 1 | 2006 | 4227 | 0.030 |
Why?
|
Syndrome | 1 | 2020 | 3271 | 0.030 |
Why?
|
Carotid Stenosis | 1 | 2001 | 859 | 0.030 |
Why?
|
Positron-Emission Tomography | 1 | 2009 | 6585 | 0.030 |
Why?
|
Glutaryl-CoA Dehydrogenase | 1 | 2012 | 19 | 0.030 |
Why?
|
Genes, X-Linked | 1 | 2013 | 127 | 0.030 |
Why?
|
Abnormalities, Multiple | 1 | 2020 | 1423 | 0.030 |
Why?
|
Muscular Diseases | 1 | 2017 | 552 | 0.030 |
Why?
|
Disease Progression | 1 | 2009 | 13511 | 0.030 |
Why?
|
DNA Copy Number Variations | 1 | 2021 | 2024 | 0.020 |
Why?
|
Pedigree | 1 | 2020 | 4537 | 0.020 |
Why?
|
Adrenoleukodystrophy | 1 | 2014 | 143 | 0.020 |
Why?
|
Mutation, Missense | 1 | 2021 | 2567 | 0.020 |
Why?
|
Adult | 6 | 2020 | 221119 | 0.020 |
Why?
|
Metabolic Diseases | 1 | 2018 | 680 | 0.020 |
Why?
|
Magnetic Resonance Imaging | 3 | 2017 | 36415 | 0.020 |
Why?
|
Delphi Technique | 1 | 2014 | 848 | 0.020 |
Why?
|
Lipotropic Agents | 1 | 2010 | 13 | 0.020 |
Why?
|
Leukocytes | 1 | 2018 | 2025 | 0.020 |
Why?
|
Single-Cell Analysis | 1 | 2021 | 2451 | 0.020 |
Why?
|
North America | 1 | 2013 | 1284 | 0.020 |
Why?
|
Electroencephalography | 2 | 2018 | 6242 | 0.020 |
Why?
|
Randomized Controlled Trials as Topic | 1 | 2006 | 10218 | 0.020 |
Why?
|
Alleles | 1 | 2020 | 6857 | 0.020 |
Why?
|
Genomic Imprinting | 1 | 2010 | 323 | 0.020 |
Why?
|
Fibroblasts | 1 | 2018 | 4137 | 0.020 |
Why?
|
Gene Duplication | 1 | 2008 | 314 | 0.020 |
Why?
|
Disease Management | 1 | 2017 | 2507 | 0.020 |
Why?
|
Placebos | 1 | 2010 | 1666 | 0.020 |
Why?
|
Statistics, Nonparametric | 1 | 2011 | 2854 | 0.020 |
Why?
|
Immunohistochemistry | 1 | 2018 | 11067 | 0.020 |
Why?
|
Consensus | 1 | 2014 | 3134 | 0.020 |
Why?
|
Drug Combinations | 1 | 2010 | 2048 | 0.010 |
Why?
|
Chromosome Deletion | 1 | 2008 | 1386 | 0.010 |
Why?
|
Gene Expression Regulation | 1 | 2021 | 11856 | 0.010 |
Why?
|
Evidence-Based Medicine | 1 | 2014 | 3691 | 0.010 |
Why?
|
Data Collection | 1 | 2011 | 3320 | 0.010 |
Why?
|
Case-Control Studies | 1 | 2019 | 22174 | 0.010 |
Why?
|
Diffusion Magnetic Resonance Imaging | 1 | 2012 | 2787 | 0.010 |
Why?
|
Genetic Testing | 1 | 2013 | 3537 | 0.010 |
Why?
|
Intracranial Arteriosclerosis | 1 | 2001 | 138 | 0.010 |
Why?
|
Middle Aged | 2 | 2020 | 220853 | 0.010 |
Why?
|
Carotid Artery, Internal | 1 | 2001 | 445 | 0.010 |
Why?
|
Treatment Outcome | 2 | 2014 | 64681 | 0.010 |
Why?
|
Pregnancy | 1 | 2017 | 29893 | 0.010 |
Why?
|
Longitudinal Studies | 1 | 2011 | 14610 | 0.010 |
Why?
|
Magnetic Resonance Angiography | 1 | 2001 | 1432 | 0.010 |
Why?
|
Infant, Newborn | 1 | 2014 | 26199 | 0.010 |
Why?
|
Radiography | 1 | 2004 | 6974 | 0.010 |
Why?
|
Retrospective Studies | 1 | 2013 | 80674 | 0.000 |
Why?
|